Genopathy
Gene-Disorder Association · Article
Gene
MYP16
Myopia 16
Disorder
Myopia 16, Autosomal Dominant
First reported 1979
Key publication · disorder Night blindness, characteristic facies, and skeletal abnormalities in two brothers.Journal of medical genetics · 1979
Manually curated
Association Review

In brief

The association between MYP16 (Myopia 16) and Myopia 16, Autosomal Dominant is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
Myopia 16, Autosomal Dominant

The disorder

5 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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04
Provenance

References & sources

1 reference

Every source and publication cited across this dossier, as one numbered reference list.

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